ALS, also known as Lou Gehrig’s Disease, is largely considered fatal and has few treatments to improve the quality of life. The ALS Association is committed to helping more people understand the impact that this devastating disease has on individuals and families nationwide.
Established in 1985, The ALS Association is the only national non-profit organization fighting Lou Gehrig’s Disease on every front. By leading the way in global research, providing assistance for people with ALS through a nationwide network of chapters, coordinating multidisciplinary care through certified clinical care centers, and fostering government partnerships, The Association builds hope and enhances quality of life while aggressively searching for new treatments and a cure.
May is ALS Awareness Month. To do our part in amplifying the mission of the ALS Association, we are giving away TWO ALS Association BowTies to those individuals who help us spread the word the most! The ALS BowTie design represents hope, with the notion that there is light at the end of the tunnel.
SHARE and RETWEET all BowTie Cause posts about ALS Awareness month.
The winners will be announced on Friday, May 30th!
Help us spread the word about this fatal disease and show our solidarity with those who need our support! Get #TiedToACause